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I C Lloyd

Showing results (31-40 of 48) with videos related to

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Journal of Pediatric Ophthalmology and Strabismus|July 31, 2010
Clinical review of periorbital capillary hemangioma of infancyAssad Jalil, Anna Maino, Rajan Bhojwani, et al.
Ophthalmic Genetics|December 29, 2004
Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesisS M Quinn, G C M Black, S Biswas, et al.
Journal of Medical Genetics|March 2, 1999
A mutation in the RIEG1 gene associated with Peters' anomalyW Doward, R Perveen, I C Lloyd, et al.
Eye (London, England)|January 1, 1992
Neonatal cataract: aetiology, pathogenesis and managementI C Lloyd, M Goss-Sampson, B G Jeffrey, et al.
Human Molecular Genetics|September 15, 1999
Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesisG C Black, R Perveen, R Bonshek, et al.
Eye (London, England)|September 24, 2011
Acute disseminated encephalomyelitis associated with optic neuritis and marked peri-papillary hemorrhagesW H Chan, I C Lloyd, J L Ashworth, et al.
The British Journal of Ophthalmology|November 26, 2002
The ophthalmic findings in Cohen syndromeK E Chandler, S Biswas, I C Lloyd, et al.
Eye (London, England)|June 8, 2013
Does the timing of treatment affect the ocular phenotype in patients with Mucopolysaccharidosis I homozygous for the L490P mutation?W H Chan, S Biswas, I C Lloyd, et al.
Eye (London, England)|November 25, 2010
Measurement of intraocular pressure in children in the UKW H Chan, I C Lloyd, J L Ashworth, et al.
The British Journal of Ophthalmology|September 1, 1995
Modulation of amblyopia therapy following early surgery for unilateral congenital cataractsI C Lloyd, J G Dowler, A Kriss, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Journal of Pediatric Ophthalmology and Strabismus|July 31, 2010
Clinical review of periorbital capillary hemangioma of infancyAssad Jalil, Anna Maino, Rajan Bhojwani, et al.
Ophthalmic Genetics|December 29, 2004
Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesisS M Quinn, G C M Black, S Biswas, et al.
Journal of Medical Genetics|March 2, 1999
A mutation in the RIEG1 gene associated with Peters' anomalyW Doward, R Perveen, I C Lloyd, et al.
Eye (London, England)|January 1, 1992
Neonatal cataract: aetiology, pathogenesis and managementI C Lloyd, M Goss-Sampson, B G Jeffrey, et al.
Human Molecular Genetics|September 15, 1999
Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesisG C Black, R Perveen, R Bonshek, et al.
Eye (London, England)|September 24, 2011
Acute disseminated encephalomyelitis associated with optic neuritis and marked peri-papillary hemorrhagesW H Chan, I C Lloyd, J L Ashworth, et al.
The British Journal of Ophthalmology|November 26, 2002
The ophthalmic findings in Cohen syndromeK E Chandler, S Biswas, I C Lloyd, et al.
Eye (London, England)|June 8, 2013
Does the timing of treatment affect the ocular phenotype in patients with Mucopolysaccharidosis I homozygous for the L490P mutation?W H Chan, S Biswas, I C Lloyd, et al.
Eye (London, England)|November 25, 2010
Measurement of intraocular pressure in children in the UKW H Chan, I C Lloyd, J L Ashworth, et al.
The British Journal of Ophthalmology|September 1, 1995
Modulation of amblyopia therapy following early surgery for unilateral congenital cataractsI C Lloyd, J G Dowler, A Kriss, et al.
Pageof 5